Inorganic Chemistry Commons^™

Modification Of A Junior-Level Capstone Course To Incorporate Scientific Writing, Bradley M. Wile

Chemistry and Biochemistry Faculty Scholarship

No abstract provided.

Catalyzed Synthesis Of Zinc Clays By Prebiotic Central Metabolites, Marcelo I. Guzman, Ruixin Zhou, Kaustuv Basu, Hyman Hartman, Christopher J. Matocha, S. Kelly Sears, Hajatollah Vali

Chemistry Faculty Publications

How primordial metabolic networks such as the reverse tricarboxylic acid (rTCA) cycle and clay mineral catalysts coevolved remains a mystery in the puzzle to understand the origin of life. While prebiotic reactions from the rTCA cycle were accomplished via photochemistry on semiconductor minerals, the synthesis of clays was demonstrated at low temperature and ambient pressure catalyzed by oxalate. Herein, the crystallization of clay minerals is catalyzed by succinate, an example of a photoproduced intermediate from central metabolism. The experiments connect the synthesis of sauconite, a model for clay minerals, to prebiotic photochemistry. We report the temperature, pH, and concentration dependence …

The Effects Of Carrier Ligands On Cisplatin Binding To Cysteine And Methionine, Adam C.R Smith

Masters Theses & Specialist Projects

We have reacted several derivatives of the anticancer drug cisplatin with N-acetyl-Lcysteine (N-AcCys) and N-acetyl-L-methionine (N-AcMet), which are two of the primary amino acid targets of platinum. NMR spectroscopy was used to monitor the reactions and determine the effect the different ligands would have on the platinum reactivity. Several of the platinum compounds were tested at pH of 4 and 7, and with platinum:amino acid ratios of 1:1, 2:1 and 1:2. Competition reactions between cysteine and methionine were done to confirm which would react with the platinum compound first. [Pt(dien)(NO3)]+ reacts faster with methionine than with cysteine at both pH …

Ruthenium-Catalyzed Dehydrogenative And Dehydrative C-H Coupling Reactions Of Arenes With Alcohols And Carbonyl Compounds, Hanbin Lee

Dissertations (1934 -)

Despite their outstanding achievements, the requirement of preformed functional groups and wasteful byproduct formation are inherent disadvantages associated with the transition metal catalyzed cross-coupling methods. Inspired by the needs for green and sustainable chemistry, transition metal catalyzed dehydrogenative and dehydrative coupling methods have been recognized as environmentally sustainable and atom economical synthetic routes for the new C-C bond formation. The catalytic activation of C-H and C-O bonds allows the formation of coupling products from ubiquitous hydrocarbon substrates by releasing hydrogen or water byproduct. However, these novel protocols require relatively harsh conditions due to their low reactivity of C-H and C-O …

Synthesis, Kinetic And Catalytic Studies Of Manganese Complexes With Corrole And Porphyrin Ligands, Haleh Jeddi

Masters Theses & Specialist Projects

High-valent transition metal-oxo intermediates play a significant role in the catalytic cycle of the ubiquitous cytochrome P450 enzymes and in biomimetic catalytic systems. In this work, manganese(III) porphyrin and corrole systems (2) were synthesized and characterized by UV-vis absorbance and 1H-NMR, matching literaturereported spectroscopic data. Manganese(V)-oxo corroles (3) and a manganese(IV)-oxo porphyrin (4) were successfully generated by chemical oxidation using mchloroperoxybenzoic acid (m-CPBA), and their oxidation reactions with organic reductants were comparatively investigated. Results from single-turnover kinetic studies indicate that in the tris(pentafluorophenyl)corrole system (3a), the active oxidizing intermediate differs in different solvents. The active oxidizing intermediate in acetonitrile is …

Effects Of Binding Affinity Between Bovine Serum Albumin And Platinum Drugs, Nathan Puckett

Masters Theses & Specialist Projects

Platinum complex drugs such as cisplatin have been used as highly successful chemotherapy drugs since the 1970s. We are interested in how the ligands attached to cisplatin analogs influences their reactivity with biologically relevant targets along with time and amount. For this study, reactions were conducted to determine the reactivity between different platinum compounds and the protein bovine serum albumin. Various platinum compounds with different ligands were reacted in varying amounts with albumin in ammonium acetate buffer for either 1 hour, 4 hours, or 24 hours. Each reaction was quenched after the designated reaction time by dialysis and the platinum …

Thickness-Properties Synergy In Organic–Inorganic Consolidated Melting-Gel Coatings For Protection Of 304 Stainless Steel In Nacl Solutions, Mario Amapricio, Andrei Jitianu, Gabriela Rodriguez, Kutaiba Al-Marzoki, Mihaela Jitianu, Jadra Mosa, Lisa C. Klein

Publications and Research

Homogeneous and crack-free methyl-substituted organic–inorganic hybrid glass coatings (thickness up to 10 μm) were deposited on AISI 304 stainless steel. Different hybrid glasses obtained fromconsolidation of the diluted melting gels with various methyltriethoxysilane (MTES)/dimethyldiethoxysilane (DMDES) ratios were evaluated considering chemical structure, coating adhesion and corrosion protection. The 70MTES/30DMDES (molar%) melting-gel coating provided improved corrosion protection for this steel due to the synergy of different properties: a highly cross-linked inorganic structure, a coating plasticity based on the hybrid network, and a good adhesion to the substrate through hydroxyl groups. Electrochemical results showa good barrier film with a passive range of 500 …

Synthesis, Structural Characterization And Catalytic Activity Of Indenyl Complexes Of Ruthenium Bearing Fluorinated Phosphine Ligands, Matthew J. Stark, Michael J. Shaw, Arghavan Fadamin, Nigam P. Rath, Eike B. Bauer

SIUE Faculty Research, Scholarship, and Creative Activity

The synthesis, characterization and catalytic activity of new ruthenium complexes of fluorinated triarylphosphines is described. The new ruthenium complexes [RuCl(ind)(PPh₃){P(p-C₆H₄CF₃)₃}] and [RuCl(ind)(PPh₃){P(3,5-C₆H₃(CF₃)₂)₃}] were synthesized in 57% and 24% isolated yield, respectively, by thermal ligand exchange of [RuCl(ind)(PPh₃)₂], where ind = indenyl ligand η⁵-C₉H₇⁻. The electronic and steric properties of the new complexes were studied through analysis of the X-ray structures and through cyclic voltammetry. The …

Photochemical Properties And Structure-Activity Relationships Of RuIi Complexes With Pyridylbenzazole Ligands As Promising Anticancer Agents, Dmytro Havrylyuk, David K. Heidary, Leona Nease, Sean Parkin, Edith C. Glazer

Chemistry Faculty Publications

Ruthenium complexes capable of light‐triggered cytotoxicity are appealing potential prodrugs for photodynamic therapy (PDT) and photoactivated chemotherapy (PACT). Two groups of (polypyridyl)Ru^II complexes with 2‐(2‐pyridyl)benzazole ligands were synthesized and investigated for their photochemical properties and anticancer activity to compare strained and unstrained systems that are likely to have different biological mechanisms of action. The structure–activity relationship was focused on the benzazole‐core bioisosterism and replacement of coligands in Ru^II complexes. Strained compounds rapidly ejected the 2‐(2‐pyridyl)benzazole ligand after light irradiation, and possessed strong toxicity in the HL‐60 cell line both under dark and light conditions. In contrast, unstrained Ru …

Synthesis And Catalytic Applications Of Non-Metal Doped Mesoporous Titania, Syed Z. Islam, Suraj R. Nagpure, Doo Young Kim, Stephen E. Rankin

Chemical and Materials Engineering Faculty Publications

Mesoporous titania (mp-TiO₂) has drawn tremendous attention for a diverse set of applications due to its high surface area, interfacial structure, and tunable combination of pore size, pore orientation, wall thickness, and pore connectivity. Its pore structure facilitates rapid diffusion of reactants and charge carriers to the photocatalytically active interface of TiO₂. However, because the large band gap of TiO₂ limits its ability to utilize visible light, non-metal doping has been extensively studied to tune the energy levels of TiO₂. While first-principles calculations support the efficacy of this approach, it is challenging to …

Enzyme–Free Uric Acid Electrochemical Sensors Using Β–Cyclodextrin Modified Carboxylic Acid Functionalized Carbon Nanotubes, Mulugeta B. Wayu, Margaret A. Schwarzmann, Samuel D. Gillespie, Michael C. Leopold

Chemistry Faculty Publications

Carboxylic acid-functionalized multi-walled carbon nanotubes (COOH-MWCNT) were modified via ultrasonication with β-cyclodextrin (β-CD) to obtain a COOH-MWCNT:β-CD nanocomposite material for the purpose of developing an enzyme-free electrochemical sensor for uric acid—a clinically relevant molecule implemented in pregnancy-induced hypertension diagnosis. The nanocomposite material is deposited onto glassy carbon electrodes and subsequently capped with layers of Nafion and Hydrothane polyurethane. The surface morphology and electronic structure of the nanocomposite material were characterized using UV–Vis, TEM, and FTIR. The performance of the electrochemical sensor was measured through direct injection of UA during amperometry. With the high surface area of the COOH-MWCNT in concert …

Effect Of Zinc Cations On The Kinetics Of Supramolecular Assembly And The Chirality Of Porphyrin J-Aggregates, A. Romeo, M. A. Castriciano, R. Zagami, G. Pollicino, L Monsù Scolaro, Robert F. Pasternack

Chemistry & Biochemistry Faculty Works

Dilute aqueous solutions of anionic meso-4-sulfonatophenyl-porphyrin (TPPS) extract zinc(ii) ions from glass or quartz surfaces at room temperature and efficiently form the corresponding metal complex (ZnTPPS). The partial or complete formation of ZnTPPS has been probed by UV/Vis spectroscopy and both static and time-resolved fluorescence. The source of zinc(ii) ions has been clearly identified through inductively coupled plasma optical emission spectrometry. The presence of increasing amounts of ZnTPPS slows down the rate of TPPS J-aggregate formation in acid solution. This influences the nucleation step and has a profound impact on the onset of chirality in these species. This evidence indicates …

Selective Atomic Layer Deposition Of Transition Metal Thin Films, Marissa Marie Kerrigan

Wayne State University Dissertations

Atomic layer deposition (ALD) affords highly conformal thin films with precise thickness control due to its self-limited growth mechanism. ALD enables the increasing demands for smaller feature sizes in microelectronics devices to be met. Area-selective ALD growth is receiving attention in the fabrication of microelectronic devices, since it can eliminate complicated etching steps from the fabrication process and minimizes expensive and toxic reagent use. Selectivity can be achieved by tailoring the surface chemistry of the precursor and substrate. To date, few area-selective ALD processes have been reported for metallic films. Thin films of cobalt metal deposited selectively are of considerable …

Ln(Ii)-Containing Cryptates: Synthesis And Properties, Akhila Nuwan Wijerathne Kuda-Wedagedara

Wayne State University Dissertations

LNII-CONTAINING CRYPTATES: SYNTHESIS AND PROPERTIES

by

AKHILA N. W. KUDA-WEDAGEDARA

May 2016

Advisor: Dr. Matthew J. Allen

Major: Chemistry

Degree: Doctor of Philosophy

Research projects described in this dissertation are focused on studying the physicochemical properties, including the photochemical, redox, and magnetic properties, of LnII-containing cryptates and how ligand structure influences metal–ligand interactions that in turn influence physicochemical properties. The results of these studies enable tailoring of the coordination properties of metal complexes that are important in applications including luminescent materials, chemical reductions, catalysis, and imaging.

A EuII-containing cryptate 2.1-EuII synthesized with an amine-rich ligand displayed bright yellow luminescence in …

Designing High Performance Overall Water Splitting Electrocatalysts From Non-Precious Metal Selenides, Abdurazag T. Swesi

Doctoral Dissertations

“The energy production has been depending mostly on fossil fuel which will be depleted someday in the near future. Aspects such as the loss of energy resources and destruction of the environment have motivated researchers for pursuing transition away from fossil fuels to renewable solar-fuels. Therefore, in order to meet the continuous increasing demand for energy, the hydrogen, with the largest energy density stored in it, can then efficiently be used in fuel cells without concern of contaminants. Water splitting reaction to generate H₂ and O₂ is one promising method of converting solar energy into fuels. The major …

Evaluation Of Earth-Abundant Monometallic And Bimetallic Complexes For Catalytic Water Splitting, Kenneth Kwame Kpogo

Wayne State University Dissertations

The development of affordable water splitting catalysts from Earth-abundant transition metal ions such as Co and Mn is of immense scientific interest. Aiming to develop an efficient water splitting catalyst, a Co(II) complex featuring an asymmetric, pentadentate quinolyl-bispyridine ligand with a phenylenediamine backbone was synthesized and characterized by spectroscopic, spectrometric, and X-ray analysis. The Co ion was selected because of its ability to undergo redox conversions from 3d5 CoIV through 3d8 CoI thereby making it a suitable catalyst that can withstand harsh structural and electronic changes during catalysis. The electrocatalytic water reduction activity of the catalyst at neutral pH gave …

Bond Length And Bond Valence Relationships For Chromium Oxides, Chromium Sulfides, Molybdenum Oxides, And Molybdenum Sulfides, J. Labrecque, F. D. Hardcastle

Journal of the Arkansas Academy of Science

Pauling determined an empirical logarithmic dependence of bond order (bond valence), s, to bond length, R, s = exp(R₀ – R/ b), where R₀ is unit bond length and b is a fitting parameter. Recently, an expression was derived for relating the b fitting parameter to theoretically derived atomic orbital exponents. With a method to calculate b, both R₀ and atomic orbital exponents can be experimentally determined through optimized fitting for Cr-O, Cr-S, Mo-O, and Mo-S. In the present study, bond length – valence relationships are found for Cr-O, Cr-S, Mo-O, and Mo-S chemical …

Bond Length And Bond Valence For Tungsten-Oxygen And Tungsten-Sulfur Bonds, F. D. Hardcastle, R. Lykins

Journal of the Arkansas Academy of Science

In 1947, Linus Pauling presented an “empirical” dependence of bond valence (s, also referred to as bond order) and bond length R: s = exp[(R₀-R)/b], where R₀ is bond length of unit valence and “b” is a fitting parameter. Recently, an expression was derived for relating the b fitting parameter to theoretically derived atomic orbital exponents. With a method to calculate b, both R₀ and atomic orbital exponents can be experimentally determined through optimized fitting for W-O and W-S bonds. In the present study, bond …

Use Of Trispyrazolemethane In The Synthesis Of Organometallic Compounds, Claire Hazelton

Undergraduate Honors Thesis Collection

Trispyrazoleborate is a negatively charged facially coordinating tridentate ligand that has been highly researched and used in many metal complexes. The related ligand trispyrazolemethane has not been widely studied due to its difficult synthesis. The objective of this project is to determine the effects of the neutral nature of the trispyrazolemethane on the metal carbonyl complexes of molybdenum and tungsten. Besides the ligand tricarbonyl complex, iodide and hydride derivatives were synthesized. All compounds were characterized with IR and HNMR.

Chalcogenide Nanocrystal Assembly: Controlling Heterogeneity And Modulating Heterointerfaces, Jessica Davis Davis

Wayne State University Dissertations

This dissertation work is focused on developing methods to facilitate charge transport in heterostructured materials that comprise a nanoscale component. Multicomponent semiconductor materials were prepared by (1) spin coating of discrete nanomaterials onto porous silicon (pSi) or (2) self-assembly. Spin-coating of colloidal quantum dot (QD) PbS solutions was employed to create prototype PbS QD based radiation detection devices using porous silicon (pSi) as an n-type support and charge transport material. These devices were initially tested as a photodetector to ascertain the possibility of their use in high energy radiation detection. Short chain thiolate ligands (4-fluorothiophenolate) and anion passivation at the …